FDA 510(k) Applications Submitted by PETER PIFERI
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K160129 | 01/20/2016 | MRII Cranial Drill and Accessories | MRI INTERVENTIONS, INC. |
| K160434 | 02/16/2016 | ClearPoint System | MRI INTERVENTIONS, INC. |
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